Allele Registry

Canonical Allele Identifier: PA2826066506

Gene: RRM2B HGNC NCBI

ClinVar Allele:

312098

ClinVar RCV:

RCV000303281

RCV000392494

RCV003766074

ClinVar Variation:

361176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Ala253Ser	CA4830963 NM_001172478.2:c.757G>T